Allele Registry

Canonical Allele Identifier: PA915969938

Gene: MFN2 HGNC NCBI

ClinVar RCV:

RCV000789370

ClinVar Variation:

637285

HGVS (amino-acid)	Matching Registered Transcripts
NP_055689.1:p.Arg94Pro	CA338462164 NM_014874.4:c.281G>C